NDC 67046-1471
Memantine Hydrochloride 5 mg tablet
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Viona Pharmaceuticals Inc.'s NDC 72578-003.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Memantine: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA090961
- On the market since
- Feb 4, 2025
- Package NDCs
67046-1471-3- Official label
- DailyMed (National Library of Medicine), updated Feb 4, 2025
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